PRODUCTS

BENZYLDIMETHYLAMINE

Benzyldimethylamine is used in the manufacture of adhesives and other chemicals.
Benzyldimethylamine is used in the preparation of bis[(N,N-dimethylamino)benzyl] selenide.
Benzyldimethylamine acts as a catalyst in the curing reaction of formulations of diglycidyl ether of bisphenol A and tetrahydrophthalic anhydride.

CAS Number: 103-83-3
EC Number: 203-149-1
MDL number: MFCD00008329
Molecular Formula: C9H13N / C6H5CH2N(CH3)2
Molecular Weight: 135.21 g/mol

SYNONYMS:
N,N-Dimethyl-1-phenylmethanamine, N,N-Dimethylbenzenemethanamine, N,N-Dimethylbenzylamine, N-Benzyldimethylamine, Dimethylbenzylamine, Benzyl-N,N-dimethylamine, N-(Phenylmethyl)dimethylamine, BDMA, Sumine 2015, Benzenemethanamine, Dabco B-16, Araldite accelerator 062, N,N-Dimethyl(phenyl)methanamine, DMBA, N,N-DIMETHYLBENZYLAMINE, 103-83-3, Benzyldimethylamine, N-Benzyldimethylamine, N,N-dimethyl-1-phenylmethanamine, Dimethylbenzylamine, BDMA, Benzenemethanamine, N,N-dimethyl-, Benzyl-N,N-dimethylamine, N-(Phenylmethyl)dimethylamine, N,N-Dimethylbenzenemethanamine, Araldite accelerator 062, N,N-Dimethyl-N-benzylamine, N-Benzyl-N,N-dimethylamine, Benzylamine, N,N-dimethyl-, Sumine 2015, N,N'-Dimethylbenzylamine, NSC 5342, Benzyl-dimethyl-amine, TYP7AXQ1YJ, DTXSID8021854, NSC-5342, NCGC00090991-02, 28262-13-7, DTXCID801854, CAS-103-83-3, CCRIS 6693, UNII-TYP7AXQ1YJ, EINECS 203-149-1, UN2619, Benzenemethanamine, dimethyl-, AI3-26794, Benzenemethamine, N,N-dimethyl-, Dabco BDMA, N,N-dimethyl-1-phenyl-methanamine, benzyldimethyl-amine, dimethylbenzyl amine, n-dimethylbenzylamine, dimethyl benzyl amine, N,N-Dmethylbenzylamne, N-benzyl dimethylamine, Benzylamine,N-dimethyl-, N,N,-dimethylbenzylamine, N,N-dimethyl benzylamine, N,N-dimethyl-benzylamine, N, N-Dimethylbenzylamine, N,N-dimethyl benzyl amine, Benzenemethanamine,dimethyl-, EC 203-149-1, dimethyl (phenylmethyl)amine, SCHEMBL15900, MLS002222342, CHEMBL45591, N,N-Dimethyl(phenyl)methanamine, NSC5342, N,N-Dimethylbenzylamine, >=99%, N,N-Dimethyl(phenyl)methanamine #, WLN: 1N1 & 1R, Tox21_113457, Tox21_200719, MFCD00008329, AKOS000120578, UN 2619, NCGC00090991-01, NCGC00090991-03, NCGC00258273-01, AC-10211, LS-13652, SMR001307284, N,N-Dimethylbenzylamine(Benzyldimethylamine), Benzyldimethylamine [UN2619], D0688, FT-0657620, NS00008694, EN300-16212, N,?N-?Dimethylbenzylamine(Benzyldimethylamine), Q424966, J-001043, J-523270, InChI=1/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H, N,N-Dimethylbenzylamine, for protein sequence analysis, >=99.5% (GC), N-Benzyl-N,N-dimethylamine, DBA, Dimethylaminomethyl-benzene, N,N-Dimethylbenzenemethanamine, N,N-Dimethylbenzylamine, DMBA, BDMA, Benzyl-dimethyl-amine, Benzyldimethylamine, Dimethylbenzylamine, DMBA, N,N'-Dimethylbenzylamine, N,N-Dimethyl-1-phenylmethanamine, N,N-Dimethyl-n-benzylamine, N,N-Dimethylbenzenemethanamine, N,N-Dimethylbenzylamine, BDMA, Dabco B-16, BENZYLDIMETHYLAMINE, Dimethylbenzylamine, N-Benzyldimethylamine, aralditeaccelerator062, N,N-Dimethylbenzylamine, N,N-BENZYLDIMETHYLAMINE, Nin-Dimethyl Benzylamine, Benzyl-N,N-dimethylamine, N,N-Dimethyl benzylamine, Araldite accelerator 062, N, N-dimethylbenzylamine, (N,N-Dimethylbenzylamine), Benzylamine, N,N-dimethyl-, N-(Phenylmethyl)dimethylamine, Benzenemethamine, N,N-dimethyl-, N,N-dimethyl-1-phenylmethanamine, Benzenemethanamine,N,N-dimethyl-, N,N-dimethyl(phenyl)methanaminium, N,N-dimethyl(phenyl)methanaminium chloride, Aralditeaccelerator062, aralditeaccelerator062, Benzenemethamine,N,N-dimethyl-, Benzenemethanamine,N,N-Chemicalbookdimethyl-, Benzylamine,N,N-dimethyl-, Benzyl-N,N-dimethylamine, DabcoB-16, N-(Phenylmethyl)dimethylamine, Benzylamine, N,N-dimethyl-, Benzyldimethylamine, Dimethylbenzylamine, N-Benzyldimethylamine, N,N-Dimethyl-N-benzylamine, N,N-Dimethylbenzylamine, N-Benzyl-N,N-dimethylamine, BDMA, Araldite accelerator 062, Benzyl-N,N-dimethylamine, N,N-Dimethylbenzenemethanamine, N-(Phenylmethyl)dimethylamine, Sumine 2015, UN 2619, Dabco BDMA, Benzenemethamine, N,N-dimethyl-, NSC 5342, N,N-Dimethylbenzylamine, N,N-Dimethyl-1-phenylmethanamine, Benzenemethanamine, N,N-dimethyl-, 103-83-3, Benzenemethanamine, N,N-dimethyl-, . 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Benzyldimethylamine is an intermediate for organic synthesis, such as synthesis of quaternary ammonium salt, also used in dehydrogenation catalyst, preservative, acid neutralizer, etc.
Benzyldimethylamine is a colorless to light yellow liquid organic compound with an aromatic odor.

Benzyldimethylamine is a colorless to light yellow liquid organic compound with an aromatic odor.
Benzyldimethylamine's chemical formula is C6H5CH2N(CH3)2 and its CAS is 103-83-3.
Benzyldimethylamine C6H5CH2N(CH3)2 contains the benzyl group, C6H5CH2, attached to a dimethylamino functional group.

Benzyldimethylamine is primarily used as a catalyst for the formation of polyurethane foams and epoxy resins.
Benzyldimethylamine is basic and undergoes quaternization with methyl iodide to produce the ammonium salt [C6H5CH2N(CH3)3] I−.
These salts are useful as phase transfer catalysts.

Benzyldimethylamine is colorless to slightly yellow transparent liquid, soluble in ethanol, soluble in hot water, slightly soluble in cold water.
Benzyldimethylamine is an aromatic amine.

Benzyldimethylamine appears as a colorless to light yellow liquid with an aromatic odor.
Benzyldimethylamine is slightly less dense than water and slightly soluble in water.
Benzyldimethylamine is the organic compound with the formula C6H5CH2N(CH3)2.

Benzyldimethylamine consists of a benzyl group, C6H5CH2, attached to a dimethylamino functional group.
Benzyldimethylamine is a colorless liquid.
Benzyldimethylamine is used as a catalyst for the formation of polyurethane foams and epoxy resins.

Benzyldimethylamine is slightly miscible with water.
Benzyldimethylamine appears as a colorless to light yellow liquid with an aromatic odor.
Benzyldimethylamine is slightly less dense than water and slightly soluble in water.

Benzyldimethylamine is slightly soluble in water.
Benzyldimethylamine can be ligated with a N-heterocyclic carbene, to produce a highly active, practical and versatile catalyst for the Heck-Mizoroki reaction.

Benzyldimethylamine is an amine catalyst that consists of a benzyl group attached to a dimethylamino group.
Benzyldimethylamine elevates your laboratory performance, a premium-grade reagent designed for precision and reliability in critical chemical processes.

This industrial-strength compound, Benzyldimethylamine, offers exceptional purity of 98+%, ensuring consistent results in your most demanding applications.

USES and APPLICATIONS of BENZYLDIMETHYLAMINE:
Benzyl Dimethyl Amine is used in adhesive and polymer manufacturing processes.
Benzyldimethylamine functions as a catalyst, curing agent, and intermediate, particularly in the production of epoxies (EP) and other polymer resins.

Certified under the Clean Water Act (CWA), Benzyldimethylamine plays a crucial role in improving the efficiency and stability of various chemical formulations.
Benzyldimethylamine is used in the manufacture of adhesives and other chemicals.

Benzyldimethylamine is used in the preparation of bis[(N,N-dimethylamino)benzyl] selenide.
Benzyldimethylamine acts as a catalyst in the curing reaction of formulations of diglycidyl ether of bisphenol A and tetrahydrophthalic anhydride.

Benzyldimethylamine undergoes directed ortho metalation with butyl lithium.
Benzyldimethylamine reacts with methyl iodide to get ammonium salt, which is used as phase transfer catalysts.
Further, Benzyldimethylamine is used as a catalyst for the formation of polyurethane foams and epoxy resins.

Benzyldimethylamine is used as an intermediate in organic synthesis, and can also be used as a dehydrogenation catalyst, preservative, acid neutralizer, etc.
Benzyldimethylamine is used in organic synthesis.

Organic synthesis intermediates, Benzyldimethylamine is used to produce new dehydrogenated halides.
Benzyldimethylamine is used catalyst, corrosion inhibitor, acid neutralizer, electron microscope slice embedding accelerator.
Benzyldimethylamine is an intermediate in organic synthesis, such as synthetic quaternary ammonium salt, etc.

Benzyldimethylamine is also used for dehydrogenation catalysts, preservatives, acid neutralizers, etc.
Benzyldimethylamine is used as the molecule has tertiary amine functionality, two of the key uses are as an epoxy-amine cure enhancement catalyst and also as a polyurethane catalyst.

Benzyldimethylamine is used in the manufacture of adhesives.
Benzyldimethylamine is used as dehydrohalogenating catalyst.
Benzyldimethylamine is used as corrosion inhibitor.

Benzyldimethylamine is used as acid neutralizer.
Benzyldimethylamine is used in potting compounds.
Benzyldimethylamine is used as cellulose modifier.

Benzyldimethylamine is used in quaternary ammonium compounds.
Benzyldimethylamine was used in the synthesis of bis[(N,N-dimethylamino)benzyl] selenide.
Benzyldimethylamine has been used as catalyst during curing reaction of formulations of diglycidyl ether of bisphenol A and tetrahydrophthalic anhydride.

Benzyldimethylamine undergoes directed ortho metalation with butyl lithium.
Benzyldimethylamine reacts with methyl iodide to get ammonium salt, which is used as phase transfer catalysts.

Further, Benzyldimethylamine is used as a catalyst for the formation of polyurethane foams and epoxy resins.
Benzyldimethylamine can also be used for the perpetration of novel electrolyte, dibenzyldimethylammonium fluoride for acylation of cellulose.

-Versatility for Industrial and Synthetic Processes of Benzyldimethylamine:
Benzyldimethylamine for industrial use is formulated to meet the demands of complex industrial processes and chemical syntheses.
Its reliable performance makes Benzyldimethylamine suitable for various applications, from material production to advanced reaction setups.

-Benzyldimethylamine is reliable Reagent for Synthesis and Reactions
Benzyldimethylaminefor synthesis and reactions is specifically designed for professionals seeking precision and consistency in their chemical applications.

Its high-purity formulation supports accurate outcomes, making Benzyldimethylamine a trusted choice for synthesis and reaction processes in research and industrial environments.

KEY BENEFITS of BENZYLDIMETHYLAMINE:
*High purity (98+%) for superior performance
*Versatile applications in organic synthesis and chemical analysis
*Effective catalyst for specific reactions
*Large 5000mL packaging for industrial-scale usage

ALTERNATIVE PARENTS of BENZYLDIMETHYLAMINE:
*Benzylamines
*Aralkylamines
*Trialkylamines
*Organopnictogen compounds
*Hydrocarbon derivatives

SUBSTITUENTS of BENZYLDIMETHYLAMINE:
*Phenylmethylamine
*Benzylamine
*Aralkylamine
*Tertiary aliphatic amine
*Tertiary amine
*Organic nitrogen compound
*Organopnictogen compound
*Hydrocarbon derivative
*Organonitrogen compound
*Amine
*Aromatic homomonocyclic compound

REACTIVITY PROFILE of BENZYLDIMETHYLAMINE:
N,N-Dimethylbenzylamine neutralizes acids on exothermic reactions to form salts plus water.
Benzyldimethylamine may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides.
Benzyldimethylamine may attack some plastics.

SYNTHESIS of BENZYLDIMETHYLAMINE:
Benzyldimethylamine can be synthesized by the Eschweiler–Clarke reaction of benzylamine.

REACTIONS of BENZYLDIMETHYLAMINE:
Benzyldimethylamine undergoes directed ortho metalation with butyl lithium:
C6H5CH2N(CH3)2 + BuLi → 2-LiC6H4CH2N(CH3)2
LiC6H4CH2N(CH3)2 + E+ → 2-EC6H4CH2N(CH3)2

Via these reactions, many derivatives are known with the formula 2-X-C6H4CH2N(CH3)2 (E = SR, PR2, etc.).
The amine is basic and undergoes quaternization with alkyl halides (e.g. hexyl bromide) to give quaternary ammonium salts:

C6H5CH2N(CH3)2 + RX → [C6H5CH2N(CH3)2R]+X−
Such salts are useful phase transfer catalysts.

PRODUCTION METHOD of BENZYLDIMETHYLAMINE:
Benzyldimethylamine is obtained by the reaction of benzyl chloride and dimethylamine.
Benzyldimethylamine can also be prepared from benzylamine, formic acid, and formaldehyde.

PREPARATION of BENZYLDIMETHYLAMINE:
Thereafter the reaction mixture was cooled in a separatory funnel while standing in a refrigerator maintained at 5°C and separated into two layers.

The upper oily layer, weighing 111.5g, was removed and steam distilled until no further oleaginous component was observed in the distillate as it came over.
The crude distillate was found to contain 103.5g of Benzyldimethylamine (76.1% of theory), 3.3g of dimethylamine and no quaternary salts.
The dimethylamine was distilled off below 29°C under atmospheric pressure from the Benzyldimethylamine (bp 82°C/18mmHg).

NOTES of BENZYLDIMETHYLAMINE:
Benzyldimethylamine has air sensitive.
Benzyldimethylamine is incompatible with strong acids, strong bases, strong oxidizing agents, strong reducing agents and carbon dioxide.

PURIFICATION METHODS of BENZYLDIMETHYLAMINE:
Dry the amine over KOH pellets and fractionate it over Zn dust in a CO2—free atmosphere.
Benzyldimethylamine has a pKa₂₅ of 8.25 in 45% aqueous EtOH.
Store Benzyldimethylamine under N2 or in a vacuum.

The picrate has m.p. 94–95 °C.
The picrolonate has m.p. 151 °C (from EtOH).
The tetraphenyl borate salt has m.p. 182–185 °C.

CHEMICAL PROPERTIES of BENZYLDIMETHYLAMINE:
Benzyldimethylamine is a colorless to light yellow flammable liquid with ammonia odor.
Benzyldimethylamine is soluble in ethanol, ether, insoluble in water.

PREPARATION of BENZYLDIMETHYLAMINE:
25% Aqueous Dimethylamine, 1088 grams
Benzyl Chloride, 126.6 grams

In the apparatus of Example 1, the benzyl chloride was added dropwise over a two-hour period to the amine (molar ratio 1 to 6) at a rate sufficient to maintain the temperature below 40°C.
Stirring was continued at room temperature for an additional hour to insure completion of the reaction denoted by the equation below.

PHYSICAL and CHEMICAL PROPERTIES of BENZYLDIMETHYLAMINE:
Molecular Weight: 135.21 g/mol
XLogP3: 2
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 2
Exact Mass: 135.104799419 g/mol
Monoisotopic Mass: 135.104799419 g/mol
Topological Polar Surface Area: 3.2Å²
Heavy Atom Count: 10

Formal Charge: 0
Complexity: 82.7
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1

Compound Is Canonicalized: Yes
CAS Min %: 98.5
CAS Max %: 100.0
Melting Point: -75.0°C
Color: Colorless to Yellow
Density: 0.9000g/mL
Boiling Point: 183.0°C to 184.0°C
Flash Point: 54°C
Infrared Spectrum: Authentic

Assay Percent Range: 98.5% min. (GC)
Linear Formula: C6H5CH2N(CH3)2
Refractive Index: 1.5000 to 1.5020
Beilstein: 12, 1019
Specific Gravity: 0.9
Solubility Information:
Solubility in water: 8g/L (20°C).
Other solubilities: soluble in alcohol,acetone,ether and toluene,
reacts with organic and inorganic acids

IUPAC Name: N,N-dimethyl-1-phenylmethanamine
Formula Weight: 135.23
Percent Purity: 99%
Physical Form: Liquid
Chemical Name or Material: N, N-Dimethylbenzylamine, 99%
Water Solubility: 2.83 g/L
logP: 1.84
logP: 1.91
logS: -1.7

pKa (Strongest Basic): 8.99
Physiological Charge: 1
Hydrogen Acceptor Count: 1
Hydrogen Donor Count: 0
Polar Surface Area: 3.24 Å²
Rotatable Bond Count: 2
Refractivity: 44.6 m³·mol⁻¹

Polarizability: 16.24 Å³
Number of Rings: 1
Bioavailability: Yes
Rule of Five: Yes
Ghose Filter: No
Veber's Rule: Yes
MDDR-like Rule: No

Chemical Formula: C9H13N
IUPAC name: benzyldimethylamine
InChI Identifier: InChI=1S/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3
InChI Key: XXBDWLFCJWSEKW-UHFFFAOYSA-N
Isomeric SMILES: CN(C)CC1=CC=CC=C1
Average Molecular Weight: 135.2062
Monoisotopic Molecular Weight: 135.104799421

CAS Number: 103-83-3
EC Number: 203-149-1
Molecular Formula: C9H13N
Molar Mass: 135.210 g·mol⁻¹
Appearance: Colourless liquid
Density: 0.91 g/cm³ at 20 °C
Melting Point: –75 °C (–103 °F; 198 K)

Boiling Point: 180 to 183 °C (356 to 361 °F; 453 to 456 K)
Solubility in Water: 1.2 g/100mL
CAS: 103-83-3
EC Number: 203-149-1
Molecular Weight: 135.21 g/mol
XLogP3: 2
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 2

Exact Mass: 135.104799419 Da
Monoisotopic Mass: 135.104799419 Da
Topological Polar Surface Area: 3.2 Å²
Heavy Atom Count: 10
Formal Charge: 0
Complexity: 82.7
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0

Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
IUPAC Name: benzyldimethylamine
InChI Key: XXBDWLFCJWSEKW-UHFFFAOYSA-N
SMILES: CN(C)CC1=CC=CC=C1

Synonym: dimethylbenzylamine
Appearance (Color): Clear colorless to pale yellow
Form: Liquid
Assay (GC): ≥98.0%
Identification (FTIR): Conforms
Refractive Index: 1.4995–1.5035 @ 20 °C
Flash Point: 54 °C (129 °F)
Refractive Index: 1.501
MDL Number: MFCD00008329

UN Number: UN2619
Sensitivity: Air sensitive
Solubility Information: Slightly miscible with water
Molecular Weight (g/mol): 135.21
Formula Weight: 135.21
Chemical Name or Material: N-Benzyldimethylamine
InChI Key: XXBDWLFCJWSEKW-UHFFFAOYSA-N
IUPAC Name: N,N-dimethyl-1-phenylmethanamine
PubChem CID: 7681

Percent Purity: ≥98%
Melting Point: –75 °C
Boiling Point: 183–184 °C
Linear Formula: C6H5CH2N(CH3)2
Quantity: 250 mL
Beilstein: 1099620
CBNumber: CB8240778
MDL Number: MFCD00026731
MOL File: 103-83-3.mol

Boiling Point: 183–184 °C 765 mm Hg (lit.)
Density: 0.9 g/mL at 25 °C (lit.)
Vapor Pressure: 2.4 hPa (20 °C)
Refractive Index: n20/D 1.501 (lit.)
Flash Point: 130 °F
Storage Temp.: Store below +30 °C
Solubility: water: soluble
pKa: pK1: 9.02 (+1) (25 °C)

Form: Liquid
Color: Clear colorless to light yellow
pH: 10 (10 g/L, H2O, 20 °C) (saturated solution)
Odor: Strong fish odor
Explosive Limit: 0.9–6.3% (V)
Water Solubility: 8 g/L (20 °C)
Sensitive: Air Sensitive
BRN: 1099620
Stability: Stable. Incompatible with strong acids, strong oxidizing agents.

LogP: 1.98 at 25 °C
CAS DataBase Reference: 103-83-3 (CAS DataBase Reference)
EWG's Food Scores: 3
FDA UNII: TYP7AXQ1YJ
NIST Chemistry Reference: Benzenemethanamine, N,N-dimethyl- (103-83-3)
EPA Substance Registry System: N,N-Dimethylbenzylamine (103-83-3)
UNSPSC Code: 12352200
NACRES: NA.26

Linear Formula: C6H5CH2N(CH3)2
CAS Number: 103-83-3
Molecular Weight: 135.21
Beilstein: 1099620
EC Number: 203-149-1
MDL Number: MFCD00008329
UNSPSC Code: 12352100
PubChem Substance ID: 24851151
NACRES: NA.22

InChI: InChI=1/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3/p+1
Molecular Formula: C9H13N
Molar Mass: 135.21
Density: 0.9 g/mL at 25 °C (lit.)
Melting Point: –75 °C
Boiling Point: 183–184 °C 765 mm Hg (lit.)
Flash Point: 130 °F
Water Solubility: 8 g/L (20 °C)
Solubility: water: soluble
Vapor Pressure: 2.4 hPa (20 °C)

Appearance: Liquid
Color: Clear colorless to light yellow
BRN: 1099620
pKa: pK1: 9.02 (+1) (25 °C)
pH: 10 (10 g/L, H2O, 20 °C)
Storage Condition: Store below +30 °C
Stability: Stable. Incompatible with strong acids, strong oxidizing agents.
Sensitive: Air Sensitive
Explosive Limit: 0.9–6.3% (V)
Refractive Index: n20/D 1.501 (lit.)

Physical and Chemical Properties
Density: 0.9
Melting Point: –75 °C
Boiling Point: 183–184 °C
Refractive Index: 1.5–1.502
Flash Point: 54 °C
Water-Soluble: 8 g/L (20 °C)
Appearance: Colorless to pale yellow clear liquid (est.)

Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity: 0.90000 @ 25.00 °C
Refractive Index: 1.50100 @ 20.00 °C
Melting Point: –10.00 °C @ 760.00 mm Hg
Boiling Point: 181.00 °C @ 760.00 mm Hg
Vapor Pressure: 0.871000 mmHg @ 25.00 °C (est.)
Flash Point: 130.00 °F TCC (54.44 °C)
logP (o/w): 1.980

Soluble In: water, 1.20E+04 mg/L @ 25 °C (exp)
water, 1.819E+04 mg/L @ 25 °C (est)
Molar Mass: 135.21 g/mol
Melting Point: -75 °C
Boiling Point: 180 - 183 °C (1013 hPa)
Boiling Range: 178 - 184 °C
Flash Point: 55 °C
Flash Point (TCC): 54 °C

Freezing Point: -75 °C
Density (25 °C): 0.897 g/cm³
Vapor Pressure (20 °C): 2.4 hPa
Steam Pressure (20 °C): 200 Pa
Refractive Index (20 °C, 589 nm): 1.5011
Refractive Index (25 °C): 1.5011
Solubility (20 °C): 8 g/L
Moisture: ≤ 0.5%
Viscosity (25 °C): 90 mPa·s

FIRST AID MEASURES of BENZYLDIMETHYLAMINE:
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available

ACCIDENTAL RELEASE MEASURES of BENZYLDIMETHYLAMINE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.

FIRE FIGHTING MEASURES of BENZYLDIMETHYLAMINE:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available

EXPOSURE CONTROLS/PERSONAL PROTECTION of BENZYLDIMETHYLAMINE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of BENZYLDIMETHYLAMINE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.

STABILITY and REACTIVITY of BENZYLDIMETHYLAMINE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available